← FDA Drug Approvals (Drugs@FDA)
SODIUM CHLORIDE 23.4%
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: FRESENIUS KABI USA · Approved 2023-07-11
Drug application
- FDA Application #
ANDA217796- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- SODIUM CHLORIDE 23.4%
- Generic name
- SODIUM CHLORIDE
- Active ingredients
- SODIUM CHLORIDE
- Dosage form
- INJECTABLE
- Route
- INJECTION
- Marketing status
- Prescription
- Sponsor
- FRESENIUS KABI USA
- Manufacturer
- Fresenius Kabi USA, LLC
- First approval
- 2023-07-11
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown